Methylenetetrahydrofolate reductase (MTHFR) polymorphisms and risk of molecularly defined subtypes of childhood acute leukemia

被引:280
作者
Wiemels, JL
Smith, RN
Taylor, GM
Eden, OB
Alexander, FE
Greaves, MF
机构
[1] Univ Edinburgh, Sch Med, Dept Publ Hlth Sci, Edinburgh EH8 9AG, Midlothian, Scotland
[2] Christie Hosp NHS Trust, Manchester M20 4BX, Lancs, England
[3] Royal Manchester Childrens NHS Trust, Acad Unit Paediat Oncol, Manchester M20 4BX, Lancs, England
[4] St Marys Hosp, Immunogenet Lab, Manchester M13 0JH, Lancs, England
[5] Univ Calif San Francisco, Dept Epidemiol & Biostat, Lab Mol Epidemiol, San Francisco, CA 94143 USA
[6] Inst Canc Res, Leukaemia Res Fund Ctr, London SW3 6JB, England
关键词
D O I
10.1073/pnas.061408298
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Low folate intake as well as alterations in folate metabolism as a result of polymorphisms in the enzyme methylenetetrahydrofolate reductase (MTHFR) have been associated with an increased incidence of neural tube defects, vascular disease, and some cancers. Polymorphic variants of MTHFR lead to enhanced thymidine pools and better quality DNA synthesis that could afford some protection from the development of leukemias, particularly those with translocations. We now report associations of MTHFR polymorphisms in three subgroups of pediatric leukemias: infant lymphoblastic or myeloblastic leukemias with MLL rearrangements and childhood lymphoblastic leukemias with either TEL-AML1 fusions or hyperdiploid karyotypes, Pediatric leukemia patients (n = 253 total) and healthy newborn controls (n = 200) were genotyped for MTHFR polymorphisms at nucleotides 677 (C -->T) and 1,298 (A -->C). A significant association for carriers of C677T was demonstrated for leukemias with MLL translocations (MLL+, n = 37) when compared with controls [adjusted odd ratios (OR) = 0.36 with a 95% confidence interval (CI) of 0.15-0.85; P = 0.017]. This protective effect was not evident for A1298C alleles (OR = 1.14). In contrast, associations for A1298C homozygotes (CC; OR = 0.26 with a 95% CI of 0.07-0.81) and C677T homozygotes (TT; OR = 0.49 with a 95% CI of 0.20-1.17) were observed for hyperdiploid leukemias (n = 138). No significant associations were evident for either polymorphism with TEL-AML1+ leukemias (n = 78), These differences in allelic associations may point to discrete attributes of the two alleles in their ability to alter folate and one-carbon metabolite pools and impact after DNA synthesis and methylation pathways, but should be viewed cautiously pending larger follow-up studies, The data provide evidence that molecularly defined subgroups of pediatric leukemias have different etiologies and also suggest a role of folate in the development of childhood leukemia.
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页码:4004 / 4009
页数:6
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